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11. The West Midland Familial Hypercholesterolaemia (FH) screening programme: Evaluating the utility of the 12 SNP polygenic risk score (PRS) across ethnic groupings

12. APOE gene testing in FH referrals – the story so far

33. Autosomal recessive hypercholesterolaemia due to homozygous ldlrap1 variants: a bristol case review

36. Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score

37. Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS)

38. Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): Expert panel recommendations and proposal of an 'FCS score'

39. Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score

40. Time To Scrap Creatinine Clearance?

43. Lipid Screening [with Reply]

44. Diagnosis of diabetes: HbA1c versus WHO criteria

45. How many patients with a monogenic diagnosis of Familial Hypercholesterolemia are currently known in UK lipid clinics?

47. The impact of swidden decline on livelihoods and ecosystem services in Southeast Asia: A review of the evidence from 1990 to 2015

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